Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Wondering


tinstar

Recommended Posts

tinstar Newbie

Good Morining new here. About 3 yrs ago my grandson was just a baby and they said that he had celiac diease. They took him to Portland to see a specialist after he was on the diet about 6 moths later and that Dr. said that all the enzymes were normal again and that maybe he did not have it. So my daughter and her husband started feeding him all this reg food again and now all the time he says he needs to throw up and that his stomach hurts. My daughter says that he is just trying to get attention. Then about 2 weeks ago my Dr. finaly found that I have Primary Biliary Cirrohis of the Liver. It is an autoimune problem that I have along awith Graves and Hoshomotos of the Thyroid. So I told my daughter to have him checked again and they said that it was alright . I think after reading all of this that maybe he does have it and so might I. I have a Black Irish background on my birth mothers side. I do not know anything about her except for a couple of thing and cannot find anything else out. Just wondering what you all think? I know that Drs are great but not always right. They were about 5 yrs late in Diagonsing me with the liver and now it is pretty bad. They say I should start thinking about the transplant list. Not for me. I just don't want the celiac to cause any problems with the grandkids. Thanks for you input. Viki :)


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



KaitiUSA Enthusiast
Good Morining new here. About 3 yrs ago my grandson was just a baby and they said that he had celiac diease. They took him to Portland to see a specialist after he was on the diet about 6 moths later and that Dr. said that all the enzymes were normal again and that maybe he did not have it. So my daughter and her husband started feeding him all this reg food again and now all the time he says he needs to throw up and that his stomach hurts. My daughter says that he is just trying to get attention. Then about 2 weeks ago my Dr. finaly found that I have Primary Biliary Cirrohis of the Liver. It is an autoimune problem that I have along awith Graves  and Hoshomotos of the Thyroid. So I told my daughter to have him checked again and they said that it was alright . I think after reading all of this that maybe he does have it and so might I. I have a Black Irish background on my birth mothers side. I do not know anything about her except for a couple of thing and cannot find anything else out. Just wondering what you all think? I know that Drs are great but not always right. They were about 5 yrs late in Diagonsing me with the liver and now it is pretty bad. They say I should start thinking about the transplant list. Not for me. I just don't want the celiac to cause any problems with the grandkids. Thanks for you input. Viki :)

<{POST_SNAPBACK}>

Celiac disease is NOT outgrown so if he was diagnosed he has it. It can cause tons of other things. Undiagnosed celiac can cause liver, gallbladder, kidney,and pancreas complications, 40-100 times more likely for cancer, diabetes, thyroid disease(very common among celiacs), osteoporosis...and thats just to name a few.

You should definitely be tested. I can give you the blood tests that need to be done if you would like. Many doctors are not up to speed on celiac unfortunately. This is just one reason why many people are not diagnosed(misdiagnosed or told they are fine) but they do have it. I have lost my trust in doctors. It is genetic so everyone in the family should be tested if one person has it. Hope this helps you out a bit.

LUAP Newbie

Drs are great but not always right.

May be doctors are great but society is not. You have a liver that is damaged. When not because of alcool, you might be interested in the fact that corn, peanuts and pistachio, contain a poison called aflatoxin b1, poison produced by the mold aspergilus flavus. Aflatoxin is well known to cause liver damages as well as cancer, and also cause b and c hepatitis type, when not killing.

On TV screen, instead of broadcast on this subject, you can see publicity about hepatitis vaccin. The position of US government is: Because there is not a lot of case of hepatitis, it shows the government handle the situation (control of aflatoxin in crops). In one word MONEY. Money first, your health is second

Knowing about aflatoxin, wouldn’t you have pay more attention when eating corn. For example, you eat fresh harvested corn and hours later, you get diarea…(why is it happening?, could it be aflatoxin?).

It’s just the same with gluten and your grand children. You might prefer the mysterious theory about celiac disease and the hla gene that touches more than 35% people. Or, if you are interested in science, you will find that there is at least two problems well explained by science with gluten. One is candida albican. The second one is Ochratoxin A. let’s have a look at the second one.

‘ochratoxin A produced predominantly by aspergillus ochraceus and penicillium verrucosum, occurs worldwide in many commodities from grains, to coffee beans, and it is implicated in urinary tumorigenesis in human and rodent. Furthermore, barley, wheat and pork products all appear to be human dietary sources of ochratoxin A’. ( national research council, Carcinogen and anticarcinogens in the human diet, p.62)

‘…although aflatoxin is the most carcinogenic substance on the planet, ochratoxin beats it ten times over in terms of its toxicity and the damage it inflicts on the human body. Despite this, the USDA does not screen for ochratoxin’. (doug kaufmann, infectious diabetes, p.35).

‘ochratoxin has been documented to cause kidney damage in laboratory animals. Scientist also believe that it cause Balkan nephropathy, a form of kidney failure common in central Europe, where ochratoxin has been found in high level in the food supply. Ochratoxin is also commonly found in the blood streams of humans. In 1996, A.V. Constantini conducted a random broad-based study in which 56 percent of his subjects tested positive for the mycotoxin, crop testing in the United states indicates that it commonly contaminates barley, corn, oats, rye, green coffee beans and peanuts. (doug kaufmann, infectious diabetes, p.90)

All that to say that gluten is bad food. Yes some family are gluten sensitive and if I had a grandkid who would have been diagnosed with that disease, that would ring a bell to me. Some people are seeing celiac disease or gluten sensitivity like a weakness (disease). When in fact, it’s a antibody reaction to a real danger. Is it the body that is stupid by attacking itself (the autoimmune disease theory)? Or is it people who are stupid keep on going eating bad food when body is showing clear evidence that it’s not good at all? that is the real question.

jenvan Collaborator

I second what kaiti said... you have to be your own and your family's advocate..as unfortunately, doctors can be mistaken! and stubborn :( it would make sense that he was testing normal about being on the diet--it would most likely confirm his diagnosis for celiac, not negate it! so talk to your daughter and share your concern... other autoimmunes are highly linked to celiac...especially thyroid. it would definitely be beneficial for you to be tested. i am so sad to hear about your liver and condition...it is so frustrating when doctors mistakes cause others to live miserably when they need not. i'm glad you're here now and wish you the best... you must have a good heart, looking out for your grandson ;)

mytummyhurts Contributor
Good Morining new here. About 3 yrs ago my grandson was just a baby and they said that he had celiac diease. They took him to Portland to see a specialist after he was on the diet about 6 moths later and that Dr. said that all the enzymes were normal again and that maybe he did not have it. So my daughter and her husband started feeding him all this reg food again and now all the time he says he needs to throw up and that his stomach hurts.

<{POST_SNAPBACK}>

Wow!! That doctor totally doesn't know what he's talking about. If he had celiac and then went gluten free then of course he wouldn't show up positive for celiac because the gluten is out of his system and he's heathy. He needs to go back on a gluten-free diet right away and stay that way for the rest of his life. celiac disease is not outgrown, many doctor falsely still believe this even though it has been disproven.

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,742
    • Most Online (within 30 mins)
      7,748

    MistyMoon
    Newest Member
    MistyMoon
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):




  • Who's Online (See full list)

    • There are no registered users currently online

  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Theresa2407
      Maybe you have a low  intolerance to Wheat.   Rye, Barley and Malt are the gluten in Celiac disease.  It has always been stated Wheat and Gluten, not just a Wheat intolerance.  Barley will keep me in bed for (2) weeks.  Gut, Migrains, Brain fog, Diahrea.  It is miserable.  And when I was a toddler the doctor would give me a malt medicine because I always had Anemia and did not grow.  Boy was he off.  But at that time the US didn't know anyone about Celiac.  This was the 1940s and 50s.  I had my first episode at 9 months and did not get a diagnosis until I was 50.  My immune system was so shot before being diagnoised, so now I live with the consequences of it. I was so upset when Manufacturers didn't want to label their products so they added barley to the product.  It was mostly the cereal industry.  3 of my favorite cereals were excluded because of this. Malt gives me a bad Gut reaction.
    • Gigi2025
      Thanks much Scott.  Well said, and heeded.   I don't have Celiac, which is fortunate.
    • Scott Adams
      Do you have the results of your endoscopy? Did you do a celiac disease blood panel before that?  Here is more info about how to do a gluten challenge for a celiac disease blood panel, or for an endoscopy: and this recent study recommends 4-6 slices of wheat bread per day:    
    • Scott Adams
      It is odd that your Tissue Transglutaminase (TTG) IgA level has bounced from the "inconclusive" range (7.9, 9.8) down to a negative level (5.3), only to climb back up near the positive threshold. This inconsistency, coupled with your ongoing symptoms of malabsorption and specific nutrient deficiencies, is a strong clinical indicator that warrants a more thorough investigation than a simple "satisfactory" sign-off. A negative blood test does not definitively rule out celiac disease, especially with such variable numbers and a classic symptomatic picture. You are absolutely right to seek a second opinion and push for a referral to a gastroenterologist. A biopsy remains the gold standard for a reason, and advocating for one is the most direct path to getting the answers you need to finally address the root cause of your suffering. Here is more info about how to do a gluten challenge for a celiac disease blood panel, or for an endoscopy: and this recent study recommends 4-6 slices of wheat bread per day:    
    • Scott Adams
      There is a distinction between gluten itself and the other chemicals and processing methods involved in modern food production. Your experience in Italy and Greece, contrasted with your reactions in the U.S., provides powerful anecdotal evidence that the problem, for some people, may not be the wheat, but the additives like potassium bromate and the industrial processing it undergoes here. The point about bromines displacing iodine and disrupting thyroid function is a significant one, explaining a potential biological mechanism for why such additives could cause systemic health issues that mimic gluten sensitivity. It's both alarming and insightful to consider that the very "watchdog" agencies meant to protect us are allowing practices banned in many other developed countries. Seeking out European flour and your caution about the high-carb, potentially diabeticgenic nature of many gluten-free products are excellent practical takeaways from your research, but I just want to mention--if you have celiac disease you need to avoid all wheat, including all wheat and gluten in Europe.
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.